Journal of the Chemical Society. Chemical communications p. 1204 - 1206 (1988)
Update date:2022-08-03
Topics: Enantioselective Experimental Kainic acid (S)-2-(Benzyloxymethyl)oxirane Route Concise
Takano, Seiichi
Iwabichi, Yoshiharu
Ogasawara, Kunio
A concise enantioselective route to (-)-kainic acid (1) from (S)-2-(benzyloxymethyl)oxirane (2) has been established by enentio- and diastereo-selective intramolecular 1,3-dipolar cyclization.
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